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SNP ID

rs143087131

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:55651129 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGACATTTGTTACTCTTCAGTCACA[C/G]CTCCCAAGATGATTGTTGACCTGTT

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

OR4S2 PubMed Links

Gene Details

Gene

OR4S2

Gene Name

olfactory receptor family 4 subfamily S member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001004059.2	226	Missense Mutation	CCT,GCT	P76A	NP_001004059.2

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